341529-16-6 Usage
Description
1-(1,1-DIFLUORO-2-PHENYL-2-TRIMETHYLSILOXY-ETHYL)-IMIDAZOLE is a chemical compound with the molecular formula C15H18F2N2OSi. It is an imidazole derivative featuring a trifluoromethyl-substituted phenyl group and a trimethylsiloxyethyl group. 1-(1,1-DIFLUORO-2-PHENYL-2-TRIMETHYLSILOXY-ETHYL)-IMIDAZOLE is often utilized in pharmaceutical research and serves as a building block for synthesizing various biologically active compounds. Its imidazole moiety also lends it potential as an antifungal agent, and it may have additional industrial applications, such as in polymer production or as a reagent in organic synthesis.
Uses
Used in Pharmaceutical Research:
1-(1,1-DIFLUORO-2-PHENYL-2-TRIMETHYLSILOXY-ETHYL)-IMIDAZOLE is used as a building block for the synthesis of biologically active compounds due to its unique chemical structure and properties.
Used in Antifungal Applications:
In the medical industry, 1-(1,1-DIFLUORO-2-PHENYL-2-TRIMETHYLSILOXY-ETHYL)-IMIDAZOLE is used as a potential antifungal agent, leveraging its imidazole moiety to combat fungal infections.
Used in Polymer Production:
1-(1,1-DIFLUORO-2-PHENYL-2-TRIMETHYLSILOXY-ETHYL)-IMIDAZOLE may be used as a component in the production of polymers, contributing to the development of new materials with specific properties.
Used as a Reagent in Organic Synthesis:
In the chemical industry, 1-(1,1-DIFLUORO-2-PHENYL-2-TRIMETHYLSILOXY-ETHYL)-IMIDAZOLE serves as a reagent in organic synthesis, facilitating the creation of a variety of organic compounds for different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 341529-16-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,1,5,2 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 341529-16:
(8*3)+(7*4)+(6*1)+(5*5)+(4*2)+(3*9)+(2*1)+(1*6)=126
126 % 10 = 6
So 341529-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H18F2N2OSi/c1-20(2,3)19-13(12-7-5-4-6-8-12)14(15,16)18-10-9-17-11-18/h4-11,13H,1-3H3
341529-16-6Relevant articles and documents
Heteroaryl-N-difluoromethyltrimethylsilanes - Versatile sources of heteroaryl-N-difluoromethyl anions in reactions with carbonyl compounds
Bissky,Staninets,Kolomeitsev,R?schenthaler
, p. 374 - 378 (2007/10/03)
An efficient procedure for synthesizing heteroaryl-N-difluoromethyltrimethylsilanes - new nucleophilic difluoromethylene synthons - from easily available N-bromodifluoromethylated heterocycles, chlorotrimethylsilane and aluminium powder in triglyme or N-methylpyrrolidinone on a preparative scale in 71-75% isolated yield is described. Heteroaryl-N-difluoromethyltrimethylsilanes and benzaldehyde react under fluoride ion catalysis to give 1-(1,1-difluor-2-hydroxy-2-phenyl-ethyl)heteroaryls, whereas for anionic heteroaryl-N-difluoromethylation of cyclohexanone a stoichiometrical mixture of heteroaryl-N-difluoromethyltrimethylsilanes and tetramethylammonium fluoride has to be used.
